Sept 13-15, 2020
Ocean Place Resort (Tentative)
Long Branch, NJ

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2016 Exhibitor List

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Exhibitor List As Of November 19, 2019

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Central Glass Germany
Cepia Sanofi
Chiral Quest Corp
Chiral Technologies, Inc.
COSMA SpA
CPC Scientific

Central Glass Germany, Booth 74 [ company website ]

Central Glass Germany is dedicated to process development, upscaling and production of active ingredients and intermediates for the pharmaceutical and cosmetics industry. It operates a FDA and EU inspected facility in Halle-Künsebeck, which it acquired from Girindus in June 2008. An experienced and highly skilled team of organic chemists and support functions, such as analytical specialists and QA/QC team, ensure success and high quality of our projects.

Cepia Sanofi, Booth 22 [ company website ]

Sanofi – CEPiA Sales is a Sanofi activity dedicated to contract manufacturing services. By employing its exhaustive industrial resources and other resources expected of big pharma, CEPiA provides its clients with “fast to market” solutions. CEPiA offers API and custom synthesis expertise in both small and large molecule chemistry from lab scale through commercial quantities. Additionally, CEPiA offers its extensive drug product capabilities including solids, semi-solids, liquids and parenteral products in vials, pre-filled syringes and devices including formulation optimization, clinical and commercial manufacturing.

Chiral Quest Corp, Booth 85 [ company website ]

Chiral Quest was founded in 2000 and moved operations to China in 2009. We acquired Jiangxi Long Life Biopharmaceuticals Co. Ltd in May 2012. Our headquarters and R&D centre is in Suzhou, with commercial scale manufacture in Jiangxi Province. Chiral Quest has expertise in asymmetric hydrogenation, multi-step synthesis and cryogenic reactions. The company has successfully developed and scaled up many processes for the commercial manufacture of API intermediates. In 2013 Chiral Quest filed USDMF’s for Duloxetine and Sitagliptin intermediates. The capacity of our manufacturing site is over 310,000 L, including 12 pressure vessels for hydrogenation.

Chiral Quest has expertise in asymmetric hydrogenation, multi-step synthesis and cryogenic reactions. The company has successfully developed and scaled up many processes for the commercial manufacture of API intermediates. In 2013 Chiral Quest filed USDMF’s for Duloxetine and Sitagliptin intermediates. The capacity of our manufacturing site is over 310,000 L, including 12 pressure vessels for hydrogenation.

Chiral Technologies, Inc., Booth 64 [ company website ]

Chiral Technologies, Inc. (CTI) is the market leader in the area of enantioselective chromatography. Together with Daicel Corporation, we support all stages of the single-enantiomer drug development process from preclinical studies to commercial drug development. We offer a full range of chiral HPLC and SFC chromatography columns for analytical, semi-preparative and preparative separations. To accelerate drug development efforts, we provide the enantioselective resolution of quantities ranging from 200 milligrams to 200 kilograms of chiral compounds, under cGMP if required. We also provide process development and pilot studies for the manufacture of chiral intermediates of approved drugs.

COSMA SpA, Booth 26

COSMA SpA (founded 1977), located in Italy, manufactures Active Pharmaceutical Ingredients for a large number of clients, mainly in regulated markets, including US, Europe and Japan. The plant includes industrial production blocks with a capacity of 140 m3 and a pilot manufacturing unit. Cosma produces both generic API and custom molecules, with a proven expertise in the development of innovative and patentable processes. Contact us at info@cfm-group.it to set up a meeting.

CPC Scientific, Booth 80 [ company website ]

CPC Scientific is a global provider of high-quality cGMP and custom peptides to researchers and pharmaceutical companies. We serve customers from early drug discovery stages through clinical trials to commercial manufacturing. CPC Scientific operates one of the largest peptide production facilities in the world so we have the capacity to handle multiple GMP projects concurrently. With our emphasis on technology, innovation, and quality, we are proud to have a US FDA inspected GMP facility, ISO 9001, and ISO 13485 certification, a claim few companies in the world can make.